Guide for intravascular device
20230241355 · 2023-08-03
Inventors
Cpc classification
A61M25/0102
HUMAN NECESSITIES
A61M25/0113
HUMAN NECESSITIES
International classification
Abstract
A device guide includes a distal portion configured for insertion through a guide catheter so as to extend out of a distal end of the guide catheter into a branch blood vessel. The distal portion of the device guide has a semi-tubular shape chosen so as to guide an intravascular device inserted through the guide catheter into the branch blood vessel
Claims
1. A device guide, comprising a distal portion configured for insertion through a guide catheter so as to extend out of a distal end of the guide catheter into a branch blood vessel, wherein the distal portion of the device guide has a semi-tubular shape chosen so as to guide an intravascular device inserted through the guide catheter into the branch blood vessel.
2. The device guide according to claim 1, and comprising an insertion rod, which is connected to a proximal end of the distal portion and is configured to push the distal portion of the device guide through the guide catheter.
3. The device guide according to claim 1, wherein the distal portion comprises a tube, which has a longitudinal cut and is configured to open along the longitudinal cut.
4. The device guide according to claim 1, wherein the distal portion has a hemi-cylindrical form.
5. The device guide according to claim 4, wherein the hemi-cylindrical form is closed around no more than 180° of a circumference of the hemi-cylindrical form.
6. The device guide according to claim 4, wherein the distal portion comprises a rounded distal tip.
7. The device guide according to claim 4, wherein the distal portion comprises one or more flexible rings extending over an open side of the distal portion.
8. The device guide according to claim 1, wherein the distal portion comprises a canted proximal end.
9. The device guide according to claim 1, wherein the distal portion has a hole in a distal end thereof, configured for passage of the intravascular device through the hole.
10. The device guide according to claim 1, wherein the distal portion has a slit in a distal end thereof.
11. The device guide according to claim 1, wherein the distal portion comprises an upward-pointing beak at a distal tip of the distal portion.
12. The device guide according to claim 1, wherein the distal portion comprises a downward-pointing beak at a distal tip of the distal portion.
13. A device guide, comprising a distal portion configured for insertion through a guide catheter into a blood vessel and having a semi-tubular shape chosen so as to guide an intravascular device inserted through the guide catheter into the blood vessel, wherein the distal portion has a hemi-cylindrical form and comprises a semicircular covering extending over an open side of the hemi-cylindrical form.
14. The device guide according to claim 13, comprising an insertion rod, which is connected to a proximal end of the distal portion, wherein the insertion rod is configured to push the distal portion of the device guide through the guide catheter.
15. The device guide according to claim 13, wherein the hemi-cylindrical form is closed around no more than 180° of a circumference of the hemi-cylindrical form.
16. The device guide according to claim 13, wherein the distal portion comprises a rounded distal tip.
17. The device guide according to claim 13, wherein the distal portion comprises a canted proximal end.
18. The device guide according to claim 13, wherein the distal portion has a hole in a distal end thereof, configured for passage of the intravascular device through the hole.
19. The device guide according to claim 13, wherein the distal portion has a slit in a distal end thereof.
20. The device guide according to claim 13, wherein the distal portion comprises a beak at a distal tip of the distal portion.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
[0018]
[0019]
DETAILED DESCRIPTION OF EMBODIMENTS
[0020] Embodiments of the present invention that are described hereinbelow provide solutions to the problems that are encountered in insertion of invasive device through tightly-curved and narrow lumens. These solutions are particularly effective in vascular catheterization, and certain embodiments are described below with reference particularly to catheterization of the coronary arteries. The principles of the present invention, however, may alternatively be applied in invasive procedures involving other sorts of physiological lumens.
[0021] In the disclosed embodiments, a device guide is inserted through a main guide catheter and is extended out of the distal end of the guide catheter into a branch artery, such as a coronary artery. The distal portion of the device guide has a radial opening extending along the length of the distal portion. A guide wire, treatment catheter or other device is then inserted through the guide catheter and passes out into the branch artery via the device guide, typically through the radial opening of the distal portion of the device guide.
[0022] For example, in some embodiments the distal portion of the guide may have a semi-tubular form. The term “semi-tubular,” as used in the context of the present patent application, means a shape defined by cutting away a longitudinal section of a hollow, cylindrical tube. One example of a semi-tubular from is a hemi-cylinder, with a circumferential extent of 180°, but other semi-tubular forms, of greater or smaller circumferential extent and shapes that are not strictly cylindrical in profile, may similarly be used in embodiments of the present invention.
[0023] This design of the device guide is advantageous in that the guide occupies relatively little space in the lumen of the guide catheter and when extended into the coronary arteries—roughly half the space occupied by a cylindrical guide of similar dimensions. Therefore, by comparison with solutions known in the art, this sort of device guide enables the cardiologist to insert intravascular devices of relatively greater diameter through the guide catheter and through the device guide and with greater ease. Furthermore, the opening of the distal portion of the device guide may be rotated so that devices passed through the guide enter curved arteries in the desired direction.
[0024] Furthermore, the shape of the device guide makes it possible to locate the device guide at some distance outside a side branch into which an intravascular device is to be inserted, and still permit the device to be inserted via the open side of the device guide. This option is generally not feasible when tubular extensions of the guide catheter are used.
[0025] In addition, the semi-tubular shape of the device guide allows blood to freely flow into a coronary artery in which the device guide is placed (whereas tubular extensions may block the artery). Freer blood flow reduces the risk of turbulence, which may lead to clotting, and also reduces or eliminates angina and risks of possible arrhythmias due to lack of blood flow into the coronaries.
[0026]
[0027] An intravascular device 32, such as a guidewire and/or treatment catheter, is then passed through catheter 20 and through guide 30 to a treatment site in artery 24. Guide 30 has a semi-tubular shape, with an opening extending along its length, and may be rotated so that this open side faces in the desired direction relative to the curvature of artery 24 (i.e., downward in the view shown in
[0028] The figures that follow show a range of possible designs of guide 30, in accordance with various embodiments of the present invention. These designs are shown by way of example and not limitation. For the sake of clarity, each guide is marked with a different indicator number, but any of them may take the place of guide 30 in the embodiment shown in
[0029]
[0030] Distal portion 42 is connected at its proximal end to an insertion rod 44, which is used to push the distal portion of guide 40 through guide catheter 20. (The other device guides shown below have similar insertion rods.) Rod 44 typically comprises a semi-rigid, kink-resistant resilient strip, made from a suitable biocompatible metal, such as stainless steel 302. This geometry enables the use of “rapid exchange” delivery systems and techniques, as well as “over the wire” techniques. Distal portion 42 is typically 20 mm long and has an outer diameter in the range of 1.7-2.3 mm. The overall length of device guide 40 may be on the order of 145 cm. Other lengths and diameters are possible, depending on the anatomy of the treated lumen.
[0031]
[0032] Radiopaque markers, containing metal of high atomic number, for example (not shown in the figure), may be embedded in guide 50 to facilitate visualization under X-ray imaging. These markers may be located in the distal part, proximal part, and/or along the length of device guide 50 in order both to locate the distal part and to indicate its orientation in three dimensions.
[0033]
[0034]
[0035]
[0036]
[0037]
[0038]
[0039]
[0040]
[0041] The use of an upward- or downward-pointing beak, with or without hole 102 (as in
[0042] Various methods can be used to produce the sorts of devices that are described above. For example, laser micro-cutting can be used to cut a metal or plastic tube to create the desired semi-tubular shape. Cuts, such as radial slits, may also be made within the device to enhance flexibility in certain segments or to permit insertion of radiopaque markers. After cutting, the tube may be overmolded with an elastic polymer.
[0043] Alternatively, a flexible wire, such as a Nitinol wire having a diameter in the range of 0.15-0.6 mm, for instance, may be formed and set in the desired shape of the device, for example bent in a curved, zigzag pattern that defines the desired shape. The wire may then be overmolded with an elastic polymer to create the final, smooth shape.
[0044] It will be appreciated that the embodiments described above are cited by way of example, and that the present invention is not limited to what has been particularly shown and described hereinabove. Rather, the scope of the present invention includes both combinations and subcombinations of the various features described hereinabove, as well as variations and modifications thereof which would occur to persons skilled in the art upon reading the foregoing description and which are not disclosed in the prior art.